149691
Thiazolidine
95%
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About This Item
Empirical Formula (Hill Notation):
C3H7NS
CAS Number:
Molecular Weight:
89.16
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
208-002-5
MDL number:
Assay:
95%
Form:
liquid
InChI key
OGYGFUAIIOPWQD-UHFFFAOYSA-N
InChI
1S/C3H7NS/c1-2-5-3-4-1/h4H,1-3H2
SMILES string
C1CSCN1
assay
95%
form
liquid
refractive index
n20/D 1.5508 (lit.)
bp
72-75 °C/25 mmHg (lit.)
density
1.131 g/mL at 25 °C (lit.)
functional group
thioether
Quality Level
Application
Thiazolidine was used in the synthesis of homogeneous penicillamine disulphide cross-linked polypeptides.
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David Pertuit et al.
Phytochemistry, 139, 81-87 (2017-04-23)
Phytochemical investigations of the roots of Spergularia marginata had led to the isolation of four previously undescribed triterpenoid saponins, a known one and one spinasterol glycoside. Their structures were established by extensive NMR and mass spectroscopic techniques as 3-O-β-D-glucuronopyranosyl echinocystic
David Pertuit et al.
Phytochemistry, 152, 182-190 (2018-05-21)
Eight undescribed triterpenoid saponins together with a known one, and two undescribed sesquiterpene glycosides were isolated from root's barks of Eriocoelum microspermum. Their structures were elucidated by spectroscopic methods including 1D and 2D experiments in combinaison with mass spectrometry as
Mark D Ericson et al.
Tetrahedron letters, 54(26), doi:10-doi:10 (2013-12-19)
The syntheses of homogeneous penicillamine disulfide cross-linked polypeptides are reported. Dodecapeptides containing N-terminal, C-terminal, or N- and C-terminal Pen were serially ligated into 36 amino acid polypeptides linked through Cys-Pen, Pen-Cys or Pen-Pen disulfide bonds. Critical to the syntheses was
Sinem Aslan Erdem et al.
Phytochemistry, 110, 160-165 (2014-12-20)
Four new oleanane-type saponins 3-O-α-L-rhamnopyranosyl-(1 → 4)-β-D-glucuronopyranosyl-22-O-β,β-dimethylacryloylA1-barrigenol (1), 3-O-α-L-rhamnopyranosyl-(1 → 4)-β-D-glucuronopyranosyl-22-O-angeloylA1-barrigenol (2), 3-O-β-D-glucopyranosyl-(1 → 2)-[β-D-glucopyranosyl-(1 → 6)]-β-D-glucopyranosyl-21,22,28-O-triacetyl-(3β,21β,22α)-olean-12-en-16-one (3), and 3-O-β-D-glucopyranosyl-(1 → 2)-glucopyranosyl-22-O-β-D-glucopyranosylsteganogenin (4), along with the known 3-O-β-D-galactopyranosyl-(1 → 2)-[α-L-arabinopyranosyl-(1 → 3)]-β-D-glucuronopyranosyl-22-O-angeloylA1-barrigenol and 3-O-α-L-rhamnopyranosyl-(1 → 4)-β-D-glucuronopyranosyloleanolic acid, were isolated from
David Pertuit et al.
Natural product communications, 10(6), 1005-1007 (2015-07-23)
A new aromatic compound 3,4,5-trimethoxyphenyl-1-O-(4-sulfo)-β-D-glucopyranoside (1), in addition to two triterpenoid saponins (chebuloside II, arjunoglucoside II), two triterpenes (arjunolic acid and 3-betulinic acid) and sitosterol-3-O-β-D-glucopyranoside have been isolated from the barks of Terminalia catappa. Their structures have been established on
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